The conformation and CETP inhibitory activity of [10]-dehydrogingerdione isolated from Zingiber officinale

In the course of searching for cholesteryl ester transfer protein (CETP) inhibitors from natural sources, a new type of CETP inhibitor, [10]-dehydrogingerdione ( 1 ), was isolated from the extract of rhizomes of Zingiber officinale Roscoe. By NMR spectroscopic analysis of its 1 HNMR, 13 C-NMR, and 1...

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Veröffentlicht in:Archives of pharmacal research 2011, 34(5), , pp.727-732
Hauptverfasser: Choi, Soon-Yong, Park, Gil-Soon, Lee, Sung Yoon, Kim, Ji Yeon, Kim, Young Kook
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Sprache:eng
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Zusammenfassung:In the course of searching for cholesteryl ester transfer protein (CETP) inhibitors from natural sources, a new type of CETP inhibitor, [10]-dehydrogingerdione ( 1 ), was isolated from the extract of rhizomes of Zingiber officinale Roscoe. By NMR spectroscopic analysis of its 1 HNMR, 13 C-NMR, and 1 H- 1 H COSY, HMBC, HMQC and NOESY, more precise structure, compared with its originally proposed structures, of [10]-dehydrogingerdione has been elucidated. This active compound inhibited human plasma CETP with IC 50 values of 35 μM.
ISSN:0253-6269
1976-3786
DOI:10.1007/s12272-011-0505-5